Walorczyk Stanisław
Institute of Plant Protection-National Research Institute, Władysława Wegorka 20, 60-318 Poznań, Poland.
J Chromatogr A. 2008 Oct 24;1208(1-2):202-14. doi: 10.1016/j.chroma.2008.08.068. Epub 2008 Aug 23.
This paper describes the extension and re-validation of a previously published multi-residue method to currently 140 pesticides and 4 pesticide degradation products in cereals and feedingstuffs. The pesticides were extracted using buffered QuEChERS ("quick, easy, cheap, rugged, effective and safe") method and then cleaned up using dispersive solid-phase extraction with Bondesil PSA and C18 sorbents, and optionally by a freezing-out clean-up step. The final extracts were analyzed in a single injection gas chromatographic-tandem quadrupole mass spectrometric (GC-MS/MS) acquisition method. A high degree of confidence was achieved by entering two multiple reaction monitoring transitions per compound. In this way, quantification of analytical results and unequivocal identification of pesticide residues in compliance with the recent European Union criteria could be done in a single analysis. Thorough optimization of the GC-MS/MS acquisition conditions and application of an effective clean-up procedure has resulted in a remarkable enhancement of the validation parameters. The linearity of the calibration curves was excellent in matrix-matched standards, and yielded the coefficients of determination (R(2))> or =0.99 for approximately 96% of the target analytes. Average recoveries of the pesticides spiked at 0.01mgkg(-1) into a feed mixture and wheat grain were in the range 70-120% with associated RSD values < or =20% for approximately 60% and 67% of the compounds, respectively. At the higher spiking levels of 0.05, 0.1 and 0.5mgkg(-1) average recoveries and RSDs readily met the validation criteria for nearly all the studied pesticides. Based on these results, the proposed approach has been proven to be highly efficient and suitable for routine determinations of multi-class pesticides in a range of cereal and related matrices. Up to now, 145 samples of matrices of differing complexity including cereals grain, bran, whole ears, straw, hay, feed mixtures and other samples such as malt, starch and dry vegetables have been analyzed. A total of 15 different pesticides have been detected, among which pirimiphos methyl (19 cases), deltamethrin (14 cases), tolylfluanid (5 cases), dichlofluanid (5 cases), and tebuconazole (4 cases) were the most frequently encountered ones.
本文描述了一种先前发表的多残留方法的扩展及重新验证情况,该方法目前可用于检测谷物和饲料中的140种农药及4种农药降解产物。采用缓冲型QuEChERS(“快速、简便、廉价、耐用、有效且安全”)方法提取农药,然后使用Bondesil PSA和C18吸附剂通过分散固相萃取进行净化,还可选择通过冷冻净化步骤进一步净化。最终提取物采用单针进样气相色谱 - 串联四极杆质谱(GC-MS/MS)采集方法进行分析。通过为每种化合物输入两个多反应监测转换,实现了高度的置信度。通过这种方式,可在一次分析中完成符合欧盟最新标准的分析结果定量及农药残留的确证鉴定。对GC-MS/MS采集条件的全面优化以及有效净化程序的应用显著提高了验证参数。基质匹配标准曲线的线性极佳,约96%的目标分析物的决定系数(R²)≥0.99。在饲料混合物和小麦籽粒中添加浓度为0.01mg/kg的农药,平均回收率在70% - 120%范围内,约分别有60%和67%的化合物其相对标准偏差(RSD)值≤20%。在0.05、0.1和0.5mg/kg的较高添加水平下,几乎所有研究农药的平均回收率和RSD均轻松满足验证标准。基于这些结果,所提出的方法已被证明高效且适用于一系列谷物及相关基质中多类农药的常规测定。截至目前,已分析了145个不同复杂程度的基质样品,包括谷物籽粒、麸皮、整穗、秸秆、干草、饲料混合物以及其他样品,如麦芽、淀粉和干蔬菜。共检测到15种不同农药,其中甲基嘧啶磷(19例)、溴氰菊酯(1例)、甲苯氟磺胺(5例)氟氯苯菊酯(5例)和戊唑醇(4例)是最常检测到的。